22753-80-6 Usage
Description
5-chloro-2-[(2,2,2-trifluoroethyl)amino]benzophenone is a benzophenone derivative characterized by the presence of a chloro and trifluoroethylamino group. It is known for its potential applications in various industries due to its unique chemical properties.
Uses
Used in Polymer Industry:
5-chloro-2-[(2,2,2-trifluoroethyl)amino]benzophenone is used as a photo-initiator for the prevention of UV light damage on polymer films. Its ability to absorb UV light and generate reactive species enables the protection of polymer films from degradation, discoloration, and loss of mechanical properties.
Used in Coatings Industry:
In the coatings industry, 5-chloro-2-[(2,2,2-trifluoroethyl)amino]benzophenone is utilized as a photo-initiator to enhance the curing process of UV-curable coatings. Its rapid absorption of UV light and generation of reactive species facilitate the cross-linking of polymer chains, resulting in faster curing times and improved coating performance.
Used in Ink Industry:
5-chloro-2-[(2,2,2-trifluoroethyl)amino]benzophenone is employed as a photo-initiator in the ink industry for UV-curable inks. Its ability to initiate the polymerization process upon exposure to UV light allows for quick drying and curing of inks, leading to enhanced print quality and durability.
Used in Adhesive Industry:
In the adhesive industry, 5-chloro-2-[(2,2,2-trifluoroethyl)amino]benzophenone is used as a photo-initiator for UV-curable adhesives. Its rapid curing properties upon exposure to UV light enable strong and durable bonds between various substrates, improving the overall performance of the adhesive.
Used in Dental Industry:
5-chloro-2-[(2,2,2-trifluoroethyl)amino]benzophenone is utilized as a photo-initiator in dental applications, specifically for the curing of dental resins and composites. Its ability to initiate the polymerization process upon exposure to UV light allows for quick setting and hardening of dental materials, leading to improved dental restorations and patient comfort.
Check Digit Verification of cas no
The CAS Registry Mumber 22753-80-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,5 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22753-80:
(7*2)+(6*2)+(5*7)+(4*5)+(3*3)+(2*8)+(1*0)=106
106 % 10 = 6
So 22753-80-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H11ClF3NO/c16-11-6-7-13(20-9-15(17,18)19)12(8-11)14(21)10-4-2-1-3-5-10/h1-8,20H,9H2
22753-80-6Relevant articles and documents
1-POLYHALOGENOALKYL-2-OXO-1,3-DIHYDRO-2H-1,4-BENZODIAZEPINES
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, (2014/02/11)
This invention relates to 2-oxo-1,3-dihydro-2H-1,4-dibenziodiazepines, and the 4-N-oxides thereof, having a polyfluoroalkyl radical attached at the 1-position thereof, to their use as muscle relaxants, as sedatives, an anticonvulsants, and as anti-anxiety agents and to the intermediates useful in the preparation thereof. The compounds may be prepared by N-polyfluoroalkylating the appropriately substituted 2-oxo-1,3-dihydro-2H-1,4-benzodiazepines. Alternate methods for the synthesis of the compounds of this invention are also described
